Variant report

Variant	nsv482198
Chromosome Location	chr16:75252884-75258821
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr16:75256157-75256423	K562	blood:	n/a	n/a
2	BRCA1	chr16:75258440-75258489	HepG2	liver:	n/a	n/a
3	CEBPB	chr16:75258165-75258497	HepG2	liver:	n/a	chr16:75258206-75258219 chr16:75258208-75258219 chr16:75258208-75258219
4	CEBPB	chr16:75253302-75253398	HepG2	liver:	n/a	chr16:75253345-75253356
5	CEBPB	chr16:75255636-75255767	HepG2	liver:	n/a	n/a
6	CEBPB	chr16:75258151-75258245	IMR90	lung:	n/a	chr16:75258206-75258219 chr16:75258208-75258219 chr16:75258208-75258219
7	CHD2	chr16:75258671-75258865	HepG2	liver:	n/a	n/a
8	CTCF	chr16:75258700-75258850	HMF	breast:	n/a	n/a
9	CTCF	chr16:75258760-75258910	HCPEpiC	choroid plexus:	n/a	n/a
10	CTCF	chr16:75257944-75257982	GM13977	blood:	n/a	n/a
11	CTCF	chr16:75256974-75257070	GM20000	blood:	n/a	n/a
12	CTCF	chr16:75258677-75258940	K562	blood:	n/a	n/a
13	CTCF	chr16:75258684-75258899	K562	blood:	n/a	n/a
14	CTCF	chr16:75258720-75258870	HMF	breast:	n/a	n/a
15	CTCF	chr16:75258746-75258914	K562	blood:	n/a	n/a
16	CTCF	chr16:75258740-75258890	K562	blood:	n/a	n/a
17	CTCF	chr16:75256762-75256866	Lung_OC	lung:	n/a	chr16:75256826-75256835 chr16:75256822-75256835 chr16:75256820-75256838
18	CTCF	chr16:75258726-75258940	K562	blood:	n/a	n/a
19	E2F6	chr16:75256177-75256300	K562	blood:	n/a	n/a
20	FOXA2	chr16:75255081-75255322	HepG2	liver:	n/a	n/a
21	HNF4A	chr16:75255470-75255708	HepG2	liver:	n/a	chr16:75255558-75255566 chr16:75255550-75255565 chr16:75255552-75255564 chr16:75255552-75255564 chr16:75255552-75255565 chr16:75255552-75255564 chr16:75255557-75255565
22	HNF4A	chr16:75255374-75255672	HepG2	liver:	n/a	chr16:75255558-75255566 chr16:75255550-75255565 chr16:75255552-75255564 chr16:75255552-75255564 chr16:75255552-75255565 chr16:75255552-75255564 chr16:75255557-75255565
23	HNF4G	chr16:75255410-75255713	HepG2	liver:	n/a	chr16:75255558-75255566 chr16:75255552-75255564 chr16:75255552-75255564 chr16:75255552-75255565 chr16:75255549-75255564 chr16:75255552-75255564 chr16:75255557-75255565
24	IRF1	chr16:75253701-75254078	K562	blood:	n/a	n/a
25	IRF1	chr16:75253819-75254019	K562	blood:	n/a	n/a
26	JUND	chr16:75258112-75259508	SK-N-SH	brain:	n/a	n/a
27	MAX	chr16:75256119-75256366	K562	blood:	n/a	chr16:75256248-75256258 chr16:75256247-75256258 chr16:75256249-75256256 chr16:75256248-75256257 chr16:75256250-75256259
28	MAX	chr16:75256121-75256432	K562	blood:	n/a	chr16:75256248-75256258 chr16:75256247-75256258 chr16:75256249-75256256 chr16:75256248-75256257 chr16:75256250-75256259
29	MAX	chr16:75256261-75256307	HepG2	liver:	n/a	n/a
30	MAX	chr16:75256043-75256438	K562	blood:	n/a	chr16:75256248-75256258 chr16:75256247-75256258 chr16:75256249-75256256 chr16:75256248-75256257 chr16:75256250-75256259
31	MYBL2	chr16:75256098-75256487	HepG2	liver:	n/a	n/a
32	MYC	chr16:75257912-75258077	H1-hESC	embryonic stem cell:	n/a	n/a
33	MYC	chr16:75257853-75257864	H1-hESC	embryonic stem cell:	n/a	n/a
34	MYC	chr16:75257871-75257886	H1-hESC	embryonic stem cell:	n/a	n/a
35	MYC	chr16:75256152-75256412	K562	blood:	n/a	chr16:75256248-75256258 chr16:75256247-75256258 chr16:75256249-75256256 chr16:75256248-75256257 chr16:75256250-75256259
36	NFYB	chr16:75253160-75253327	GM12878	blood:	n/a	n/a
37	NR3C1	chr16:75257250-75257629	A549	lung:	n/a	n/a
38	NR3C1	chr16:75257255-75257608	A549	lung:	n/a	n/a
39	PBX3	chr16:75258604-75259519	SK-N-SH	brain:	n/a	n/a
40	PBX3	chr16:75258615-75259490	SK-N-SH	brain:	n/a	n/a
41	PML	chr16:75258773-75259312	MCF-7	breast:	n/a	n/a
42	POLR2A	chr16:75257439-75257511	H1-hESC	embryonic stem cell:	n/a	n/a
43	POLR2A	chr16:75258443-75259081	MCF10A-Er-Src	breast:	n/a	n/a
44	POLR2A	chr16:75256897-75256932	MCF-7	breast:	n/a	n/a
45	POLR2A	chr16:75256940-75257068	ProgFib	skin:	n/a	n/a
46	POLR2A	chr16:75257117-75257150	H1-hESC	embryonic stem cell:	n/a	n/a
47	POLR2A	chr16:75256928-75257086	K562	blood:	n/a	n/a
48	POLR2A	chr16:75258341-75259395	H1-hESC	embryonic stem cell:	n/a	n/a
49	POLR2A	chr16:75258069-75258461	U87	brain:	n/a	n/a
50	POLR2A	chr16:75257848-75258061	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:75252973-75253023	AG09319	gingival:	n/a
2	chr16:75252973-75253023	AG09319	gingival:	n/a
3	chr16:75258780-75258830	HAEpiC	amniotic membrane:	n/a
4	chr16:75255590-75255640	HUVEC	blood vessel:	n/a
5	chr16:75258780-75258830	ProgFib	skin:	n/a
6	chr16:75252973-75253023	PFSK-1	brain:	n/a
7	chr16:75252973-75253023	PrEC	prostate:	n/a
8	chr16:75258780-75258830	BJ	skin:	n/a
9	chr16:75252973-75253023	HepG2	liver:	n/a
10	chr16:75255590-75255640	Caco-2	colon:	n/a
11	chr16:75255590-75255640	AoSMC	blood vessel:	n/a
12	chr16:75258780-75258830	HCM	heart:	n/a
13	chr16:75252973-75253023	GM06990	blood:	n/a
14	chr16:75258780-75258830	AG09309	skin:	n/a
15	chr16:75255590-75255640	GM12878	blood:	n/a
16	chr16:75255590-75255640	NHDF-neo	bronchial:	n/a
17	chr16:75258780-75258830	ECC-1	luminal epithelium:	n/a
18	chr16:75255590-75255640	SKMC	muscle:	n/a
19	chr16:75252973-75253023	SK-N-SH_RA	brain:	n/a
20	chr16:75252973-75253023	HUVEC	blood vessel:	n/a
21	chr16:75255590-75255640	BE2_C	brain:	n/a
22	chr16:75258780-75258830	GM12891	blood:	n/a
23	chr16:75258780-75258830	MCF10A-Er-Src	breast:	n/a
24	chr16:75252973-75253023	GM12878	blood:	n/a
25	chr16:75255590-75255640	HL-60	blood:	n/a
26	chr16:75255590-75255640	U87	brain:	n/a
27	chr16:75255590-75255640	AG09309	skin:	n/a
28	chr16:75252973-75253023	HRCEpiC	kidney:	n/a
29	chr16:75258780-75258830	HCF	heart:	n/a
30	chr16:75258780-75258830	HCPEpiC	choroid plexus:	n/a
31	chr16:75255590-75255640	GM06990	blood:	n/a
32	chr16:75252973-75253023	Hepatocyte	liver:	n/a
33	chr16:75255590-75255640	HMEC	breast:	n/a
34	chr16:75252973-75253023	NT2-D1	testis:	n/a
35	chr16:75258780-75258830	SK-N-SH	brain:	n/a
36	chr16:75255590-75255640	HCF	heart:	n/a
37	chr16:75258780-75258830	BE2_C	brain:	n/a
38	chr16:75255590-75255640	HRCEpiC	kidney:	n/a
39	chr16:75258780-75258830	HIPEpiC	eye:	n/a
40	chr16:75255590-75255640	Hepatocyte	liver:	n/a
41	chr16:75258780-75258830	GM19239	blood:	n/a
42	chr16:75258780-75258830	IMR90	lung:	fetal
43	chr16:75258780-75258830	SKMC	muscle:	n/a
44	chr16:75252973-75253023	SKMC	muscle:	n/a
45	chr16:75258780-75258830	HRCEpiC	kidney:	n/a
46	chr16:75258780-75258830	AG04449	skin:	fetal
47	chr16:75252973-75253023	T-47D	breast:	n/a
48	chr16:75258780-75258830	NHDF-neo	bronchial:	n/a
49	chr16:75252973-75253023	GM12891	blood:	n/a
50	chr16:75252973-75253023	HNPCEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr16:75251309..75253963-chr16:75256152..75258523,2	K562	blood:
2	chr16:75239031..75241821-chr16:75257003..75259072,2	MCF-7	breast:
3	chr16:75258373..75260591-chr16:75260652..75263277,2	K562	blood:
4	chr16:75239816..75243837-chr16:75256696..75260507,7	MCF-7	breast:
5	chr16:75251309..75253963-chr16:75256152..75258523,2	K562	blood:

Variant related genes	Relation type
ENSG00000240338	TF binding region
CTRB1	TF binding region
ENSG00000240338	CpG island
CTRB1	CpG island
ENSG00000240338	chromatin interactions
ENSG00000168928	chromatin interactions
ENSG00000168925	chromatin interactions

Extended variants
information (count: 388 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:388 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs199716713	chr16:75252901-75252902	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs112981559	chr16:75252902-75252903	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs1130448	chr16:75252941-75252942	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs1130449	chr16:75252942-75252943	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs1130450	chr16:75252947-75252948	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs1130452	chr16:75252948-75252949	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs1130453	chr16:75252951-75252952	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs1130454	chr16:75252956-75252957	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs201245474	chr16:75252957-75252958	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs371689386	chr16:75252967-75252968	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs375837360	chr16:75252994-75252995	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs115013485	chr16:75252995-75252996	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs370211535	chr16:75252999-75253000	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs373699068	chr16:75253001-75253002	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs570058935	chr16:75253011-75253012	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs553503419	chr16:75253022-75253023	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs570657605	chr16:75253028-75253029	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs114786191	chr16:75253039-75253040	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs539212768	chr16:75253047-75253048	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs558931262	chr16:75253050-75253051	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs556315255	chr16:75253056-75253057	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs576359647	chr16:75253060-75253061	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs541828117	chr16:75253094-75253095	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs556038074	chr16:75253140-75253141	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs368169571	chr16:75253178-75253179	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs374213915	chr16:75253186-75253187	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs572732468	chr16:75253214-75253215	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs541694572	chr16:75253216-75253217	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs184317277	chr16:75253229-75253230	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs142111383	chr16:75253243-75253244	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs545893130	chr16:75253297-75253298	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs114103184	chr16:75253304-75253305	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs531353704	chr16:75253305-75253306	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs375234628	chr16:75253307-75253308	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs369498018	chr16:75253310-75253311	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs568345510	chr16:75253312-75253313	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs188534281	chr16:75253321-75253322	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs151169459	chr16:75253323-75253324	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs140212040	chr16:75253331-75253332	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs572676884	chr16:75253346-75253347	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs539571255	chr16:75253356-75253357	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs541780418	chr16:75253358-75253359	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs556637788	chr16:75253359-75253360	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs7184411	chr16:75253370-75253371	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs573982357	chr16:75253372-75253373	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs12598363	chr16:75253380-75253381	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs574458766	chr16:75253426-75253427	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs7184591	chr16:75253435-75253436	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs572819570	chr16:75253470-75253471	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs145258774	chr16:75253484-75253485	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16702952	CNVD
Medulloblastoma	16968546	CNVD
Prostate cancer	19242612	CNVD
Cancer	22429812	CNVD
Ewing''s sarcoma	21437220	CNVD
Ewing''s sarcoma	22429812	CNVD
Melanoma	18172304	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Multiple myeloma	21628407	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	17245344	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Melanoma	22183965	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Poland''s syndrome	22110015	CNVD
Neuroblastoma	21899760	CNVD
Liver carcinoma	19366792	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	19156837	CNVD
Acute myeloid leukemia	17377590	CNVD
Breast cancer	20409316	CNVD
Hepatocellular carcinoma	16750200	CNVD
Epilepsy	20502679	CNVD

Chromatin state (count:163 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:75246800-75261000	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr16:75249400-75254000	Enhancers	Placenta	Placenta
3	chr16:75250200-75254000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr16:75251400-75256200	Weak transcription	Right Atrium	heart
5	chr16:75251600-75261600	Weak transcription	HMEC	breast
6	chr16:75252200-75253000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr16:75252200-75253200	Enhancers	Brain Anterior Caudate	brain
8	chr16:75252200-75253200	Enhancers	Brain Cingulate Gyrus	brain
9	chr16:75252200-75253400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
10	chr16:75252200-75253400	Enhancers	HSMM	muscle
11	chr16:75252200-75253600	Flanking Bivalent TSS/Enh	HepG2	liver
12	chr16:75252200-75254000	Enhancers	Brain Substantia Nigra	brain
13	chr16:75252200-75255000	Active TSS	Pancreas	Pancrea
14	chr16:75252400-75253200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr16:75252400-75253200	Enhancers	Fetal Muscle Leg	muscle
16	chr16:75252400-75253200	Enhancers	HSMMtube	muscle
17	chr16:75252400-75253400	Enhancers	Primary T helper naive cells from peripheral blood	blood
18	chr16:75252400-75253400	Enhancers	Dnd41	blood
19	chr16:75252400-75253800	Enhancers	Brain Hippocampus Middle	brain
20	chr16:75252600-75253000	Enhancers	GM12878-XiMat	blood
21	chr16:75252600-75253400	Enhancers	Brain Inferior Temporal Lobe	brain
22	chr16:75252600-75253600	Enhancers	Primary T cells fromperipheralblood	blood
23	chr16:75252600-75253600	Enhancers	Fetal Muscle Trunk	muscle
24	chr16:75252600-75254000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
25	chr16:75252600-75258200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr16:75252600-75262000	Weak transcription	Brain Angular Gyrus	brain
27	chr16:75252800-75253600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
28	chr16:75252800-75253600	Enhancers	Primary T helper cells fromperipheralblood	blood
29	chr16:75252800-75253600	Active TSS	Pancreatic Islets	Pancreatic Islet
30	chr16:75252800-75254600	Enhancers	Fetal Thymus	thymus
31	chr16:75253000-75253200	Enhancers	Primary T cells from cord blood	blood
32	chr16:75253000-75253200	Flanking Active TSS	GM12878-XiMat	blood
33	chr16:75253000-75253400	Enhancers	Thymus	Thymus
34	chr16:75253000-75253600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
35	chr16:75253000-75253600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
36	chr16:75253000-75253600	Enhancers	Primary T helper cells PMA-I stimulated	--
37	chr16:75253000-75253600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
38	chr16:75253000-75253600	Enhancers	Primary T killer memory cells from peripheral blood	blood
39	chr16:75253000-75253800	Enhancers	Primary B cells from cord blood	blood
40	chr16:75253000-75254000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
41	chr16:75253000-75254600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
42	chr16:75253000-75256000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr16:75253200-75253600	Enhancers	GM12878-XiMat	blood
44	chr16:75253200-75254000	Enhancers	Fetal Brain Male	brain
45	chr16:75253200-75256000	Weak transcription	Fetal Muscle Leg	muscle
46	chr16:75253200-75256200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr16:75253200-75261800	Weak transcription	Brain Anterior Caudate	brain
48	chr16:75253200-75263400	Weak transcription	HSMMtube	muscle
49	chr16:75253400-75253600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr16:75253400-75253800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain

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